Subcutaneous Tissue Expander

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K790842 ↗

FDA Product Code

LCJ

Device Class

U

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• 2 Fr Kelman Chamber Maintainer

  Class II

  FDA 510(k) K792096 Active Cleared 16 Nov 1979

• Radovan Subcutaneous Tissue Expander

  Unclassified

  FDA 510(k) K771224 Active Cleared 11 Oct 1977

• Mishler 2 Chamb Flushing Valve, Anti-Syph

  Class II

  FDA 510(k) K760785 Active Cleared 1 Nov 1976

• Valve, Standard Model Pudenze Flushing

  Class II

  FDA 510(k) K760501 Active Cleared 30 Aug 1976

• Mishler 2 Chamb Flushing Valve, Stand

  Class II

  FDA 510(k) K760784 Active Cleared 1 Nov 1976

• T-Tube Drain, Round

  Class I

  FDA 510(k) K760778 Active Cleared 3 Nov 1976

See all devices from Heyer Schulte Corp. →